A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5846589



Internal ID22621524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38109689..38116789hg38UCSC Ensembl
chr7:38149291..38156391hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg387101
hg197101
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17506345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5846589
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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